Using life cycle assessment for municipal solid waste management in Tehran Municipality Region 20

Background: Due to the lack of a proper waste management system, Tehran Municipality Region 20 is facing economic and environmental problems such as the high costs of a disposal system and source pollution. Life cycle assessment (LCA) is a method for collecting and evaluating the inputs, outputs, and potential environmental impacts of a product system throughout its life cycle. The current study purposed to provide a stable and optimized system of solid waste management in Tehran Municipality Region 20. Methods: The LCA method was used to evaluate various scenarios and compare the effects on environmental aspects of management systems. Four scenarios were defined based on existing and possible future waste management systems for this region. These scenarios were considered with different percentages for source separation, composting, recycling, and energy recovery. Results: Based on the results of this study, Scenario 4 (source separation [14%] + composting [30%] + municipal recycling facility [MRF] [20%] + energy recovery [10%] + landfilling [26%]) was found to be the option with the minimum environmental impact. In the absence of government support and sufficient funds for establishing energy recovery facilities, the third scenario (source separation [14%] + composting [30%] +MRF [20%] + landfilling [36%]) is recommended. Conclusion: The results acquired from this investigation will confirm the belief that LCA as an environmental device may be successfully used in an integrated solid waste management system (ISWMS) as a support tool for decision-making

The culm and glume anatomical study on Lolium (Poaceae) species in Iran

Lolium (Poaceae) is composed of five species in Iran that are of forage and weed importance. Culm and glume anatomy of grasses is inadequately explored. In the present study culm and glume anatomical structures of 17 population of four Lolium species is considered by use of 16 qualitative and quantitative features to distinguish Lolium species in Iran and to determine their diagnostic value. The culm cross-section showed multilayered hypodermis, ribbed or un-ribbed culm cross-sections, cuticles with different thicknesses, and the cortex with different tissues. Vascular bundles are arranged in two to more rings in the culm anatomy. Glume anatomical observations showed differences in girder attachment to vascular bundles, the outline of the cross-section, and the cortex tissue composition. The multi-variate statistical method based on culm and glume anatomical features showed that L. perenne and L. multiflorum are grouped near each other but there is more mixture between L. persicum and L. rigidum. Our findings are in agreement with the grouping pattern achieved by previous researches on leaf anatomy and lemma and palea micro-morphology of the same species. The molecular study by ISSR also provides support for the present study. The culm and glume anatomy of species studied provides valuable data for taxonomic purposes

Seismic design of masonry-infilled frames: A review of codified approaches

This paper reviews the approach of eleven national codes on the analysis and design of masonry-infilled frames. It is shown that, in general, codes can be divided into two groups. The first group isolates the masonry and frame members by providing gaps to minimize the interaction between them. This method ensures that the complexities involved in analyzing the structure is avoided. However, the width of the gaps recommended is different for each of the codes. The second group takes advantage of the presence of high stiffness and strength masonry infill. In this technique, an equivalent-strut modeling strategy is mostly recommended. It is shown that the strut model suggested in each of the codes is different. An attempt to obtain a generic model for masonry-infilled frame failed largely due to the existence of many behavior-influencing parameters. Finally, it is suggested to have a paradigm shift in the modeling strategy where the masonry-infilled frames are classified into different categories and a model is suggested for each of them

Isolation, cloning and molecular analysis of ag85a and tb10.4 genes from Mycobacterium tuberculosis

Background: Novel tuberculosis (TB) vaccines that aim to boost and/or replace Bacillus Calmette-Guerin (BCG) are currently in development. DNA vaccines can stimulate both humoral and cell-mediated immunity in different animal models of TB and is thought to be a promising strategy in the development of new vaccines against TB. The aim of this study was to design and construct a DNA vaccine encoding ag85a and tb10.4 fusion genes of Mycobacterium tuberculosis.Materials and Methods: tb10.4 fragment was amplified by PCR and the product was digested with restrictionenzymes. Next, it was cloned into the pcDNA3.1+ plasmid. The ag85a gene and pcDNA3.1+/tb10.4 plasmid were digested by EcoRI and BamHI restriction enzymes. Constructed vector was sequenced. The molecular analysis was done using bioinformatics software. New chimeric vector containing ag85a-tb10.4 genes were purified. Expression of pcDNA3.1+/tb10.4-ag85a plasmid was confirmed in eukaryotic cells.Results: Fragments of 297 bp for tb10.4 and 1017 bp for ag85a were observed in agarose gel electrophoresis.Alignment of ag85a-tb10.4 genome sequence with reference genes in GenBank showed exact identities that indicate correction of all cloning procedures. Transfection of eukaryotic cells with pcDNA3.1+/tb10.4-ag85a vector and existence of tb10.4-ag85a fusion gene were both confirmed with RT-PCR.Conclusion: In this study, tb10.4 and ag85a genes were isolated from Mycobacterium tuberculosis H37Rv strain and cloned into pcDNA3.1+. Also, the capability of constructed vector in producing fusion ag85a-tb10.4 protein was confirmed with RT-PCR. pcDNA3.1+/tb10.4-ag85a vector can be used for further studies in future

Analysis of Association between the Effects of Methylphenidate and DRD4 Gene Polymorphisms in Patients with Attention Deficit Hyperactivity Disorder

Background: Drug treatment is one of the most important treatments for attention deficit hyperactivity disorder (ADHD). The DRD4 gene is a transporter and receptor coding gene of dopamine and is one of the most important genes under investigation in the disorder and etiology of ADHD. In this study, the association between rs3758653 C/T and VNTR exon 3 repetition polymorphisms of the DRD4 gene and the effects of methylphenidate were investigated in patients with ADHD disorder consuming methylphenidate. Methods: The descriptive-analytical study was performed on 122 patients (5 - 18 years old) with ADHD who were treated with methylphenidate. DNA was extracted using salting out method. Subsequently, the rs3758653 polymorphism in the 5’UTR region of DRD4 gene was genotyped by PCR-RFLP method, and the VNTR fragment in exon III of DRD4 gene was investigated by electrophoresis gel on acrylamide gel method. After eight weeks from the start of drug treatment with methylphenidate, the intensity of symptoms was evaluated using the Conners scale. Finally, all data from questionnaires and information that were resulted from laboratory findings were analyzed using ANOVA and repeated measure analysis. Results: Of the 122 patients under study, 15 patients (12.3%) were responded to the drug treatment, and 107 patients (87.7%) were not responded. The significant differences were not revealed in genotype, and allele frequencies of between rs3758653 (C/T) and exon III 3’VNTR repeats polymorphisms of the DRD4 gene and responder and non-responder of ADHD groups to the drug treatment. Conclusions: The results showed that the reduction of ADHD symptoms with drug treatment is not related to DRD4 sub-types in patients with ADHD

Investigating the Role of Environmental Factors on the Survival, Stability, and Transmission of SARS-CoV-2, and Their Contribution to COVID-19 Outbreak: A Review

publishedVersio

Indicators of Quality of Care in Individuals With Traumatic Spinal Cord Injury: A Scoping Review

Study Design: Scoping review. Objectives: To identify a practical and reproducible approach to organize Quality of Care Indicators (QoCI) in individuals with traumatic spinal cord injury (TSCI). Methods: A comprehensive literature review was conducted in the Cochrane Central Register of Controlled Trials (CENTRAL) (Date: May 2018), MEDLINE (1946 to May 2018), and EMBASE (1974 to May 2018). Two independent reviewers screened 6092 records and included 262 full texts, among which 60 studies were included for qualitative analysis. We included studies, with no language restriction, containing at least 1 quality of care indicator for individuals with traumatic spinal cord injury. Each potential indicator was evaluated in an online, focused group discussion to define its categorization (healthcare system structure, medical process, and individuals with Traumatic Spinal Cord Injury related outcomes), definition, survey options, and scale. Results: A total of 87 indicators were identified from 60 studies screened using our eligibility criteria. We defined each indicator. Out of 87 indicators, 37 appraised the healthcare system structure, 30 evaluated medical processes, and 20 included individuals with TSCI related outcomes. The healthcare system structure included the impact of the cost of hospitalization and rehabilitation, as well as staff and patient perception of treatment. The medical processes included targeting physical activities for improvement of health-related outcomes and complications. Changes in motor score, functional independence, and readmission rates were reported as individuals with TSCI-related outcomes indicators. Conclusion: Indicators of quality of care in the management of individuals with TSCI are important for health policy strategists to standardize healthcare assessment, for clinicians to improve care, and for data collection efforts including registries

Bridging performance of new eco-friendly lost circulation materials

Lost circulation is one of the most important concerns of the drilling industry, causing excessive expenditure and increasing the non-productive drilling time. In this study, various lost circulation materials (LCMs) were used to control the lost circulation of two types of drilling fluids, bentonite mud and a new eco-friendly mud, named RIA-X, which has a remarkable effect on decreasing the amount of lost circulation in fractured and highly permeable reservoirs. The Bridging Material Test (BMT) apparatus was used to investigate the effectiveness of various LCMs in fractures of various sizes and to select the LCM and combination with the best performance. The use of three-dimensional fractures is one of the most notable points of this work, which makes the experimental conditions similar to those of real wells. The lost control performance of the new eco-friendly LCMs in RIA-X mud was tested in field. The outcomes show that the designed LCMs are able to control severe lost circulation that regular processes such as cementing or drilling with foam cannot deal with

Prevalence of reflux nephropathy in Iranian children with solitary kidney: results of a multi-center study

Abstract Background: Given the importance of the function of the remnant kidney in children with unilateral renal agen‑ esis and the significance of timely diagnosis and treatment of reflux nephropathy to prevent further damage to the remaining kidney, we aimed to determine the prevalence of reflux nephropathy in this subgroup of pediatric patients. Methods: In general, 274 children referred to pediatric nephrologists in different parts of Iran were evaluated, of whom 199 had solitary kidney and were included in this cross‑sectional study. The reasons for referral included urinary tract infection (UTI), abnormal renal ultrasonography, being symptomatic, and incidental screening. Demographic characteristics, including age and gender were recorded. History of UTI and presence of vesicoureteral reflux (VUR) were evaluated. Results: Of the 274 children evaluated in this study with the mean age (SD) of 4.71 (4.24) years, 199 (72.6%) had solitary kidney. Among these, 118 (59.3%) were male and 81 (60.7%) were female, 21.1% had a history of UTI, and VUR was present in 23.1%. The most common cause of referral was abnormal renal ultrasonography (40.2%), followed by incidental screening (21.1%), being symptomatic (14.1%), and UTI (5.5%). In 116 children (58.3%), the right kidneys and in 83 (41.7%) the left kidneys were absent. Besides, 14.6% of the participants had consanguineous parents and 3% had a family history of solitary kidney. Upon DMSA scan, the single kidney was scarred in 13.1%, of which only 7.5% were associated with VUR. In addition, proteinuria and hematuria were observed in 6.5% and 1.5% of children, respectively. Conclusions: The prevalence of reflux nephropathy was 7.5% in children with solitary kidney with a male predomi‑ nance. Given the relatively high prevalence of reflux nephropathy in these children, screening for VUR in the remnant kidney appears to be essential in this population. Keywords: Vesicoureteral reflux, Nephropathy, Children, Solitary kidney, Renal agenesi